Naloxone Hydrochloride
- Product NDC
- 50090-3294
- 11-digit product format
- 500903294
- Labeler code
- 50090
- Product ID
- 50090-3294_f018b037-01eb-493c-a2f8-7ff7515bab00
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Naloxone Hydrochloride
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- A-S Medication Solutions
- Application
- ANDA208871
- Marketing category
- ANDA
- Marketing start
- 2017-02-28
- Marketing end
- 0000-00-00
- Substance
- NALOXONE HYDROCHLORIDE
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Opioid Antagonist [EPC],Opioid Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-3294-0 | 50090329400 | 10 VIAL, SINGLE-DOSE in 1 CARTON (50090-3294-0) > 1 mL in 1 VIAL, SINGLE-DOSE | 2017-12-01 | 0000-00-00 | No | No | Current |